Sodium Hydroxide → 7-(4-Carboxy-phenoxy)-3,4-dihydro-1H-isoquinoline-2-carboxylic acid benzyl ester
反応式
[OH-].[Na+].[CH2:3]([O:10][C:11]([N:13]1[CH2:22][CH2:21][C:20]2[C:15](=[CH:16][C:17]([O:23][C:24]3[CH:29]=[CH:28][C:27]([C:30]([O:32]CC)=[O:31])=[CH:26][CH:25]=3)=[CH:18][CH:19]=2)[CH2:14]1)=[O:12])[C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1>C(O)C>[CH2:3]([O:10][C:11]([N:13]1[CH2:22][CH2:21][C:20]2[C:15](=[CH:16][C:17]([O:23][C:24]3[CH:25]=[CH:26][C:27]([C:30]([OH:32])=[O:31])=[CH:28][CH:29]=3)=[CH:18][CH:19]=2)[CH2:14]1)=[O:12])[C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1参加物
4
反応条件
- 温度
- 45 °C
実験手順
Sodium hydroxide (0.73 g dissolved in 25 mL water) is added to a solution of 7-(4-ethoxycarbonyl-phenoxy)-3,4-dihydro-1H-isoquinoline-2-carboxylic acid benzyl ester (3.00 g) in ethanol (100 mL). The resulting suspension is stirred at 45° C. overnight. The solution is concentrated and the aqueous residue is adjusted to pH value 2-3 using 1 M hydrochloric acid. Then dichloromethane is added and the mixture is stirred for 10 min. The organic phase is separated and the aqueous phase is extracted with dichloromethane twice. The combined organic phases are dried (Na2SO4) and concentrated. The residue is purified by chromatography on silica gel (petrol ether/ethyl acetate/acetic acid 50:50:0.5) to furnish the title compound as an oil.